Holaday D A, Fiserova-Bergerova V
Anesth Analg. 1976 Nov-Dec;55(6):853-62. doi: 10.1213/00000539-197611000-00024.
1-bromo-1,2,2-trifluorocyclobutane (42M-9) has physical properties similar to those of methoxyflurane and has been suggested for use as an anesthetic agent. Its MAC value, predicted from its lipid solubility, is 0.26 percent. No clinically significant changes were observed in cardiovascular or respiratory function or in clinical laboratory tests. Ventricular dysrhythmias were not seen in this study at analgesic concentrations in contrast to those reported at anesthetic concentrations by others. Pulmonary uptake was high and wash-out was slow. The total amount exhaled comprised 60 percent of the dose. Fluorine, equivalent to 11 percent of total uptake, was rapidly excreted in urine as nonvolatile fluorinated metabolites. An additional 9 percent of 42M-9 was degraded to fluroide and excreted in urine. Since an amount of fluoride equivalent to that excreted in the urine tends to be deposited in the skeleton, approximately 29 percent of uptake may possibly be accounted for as metabolites. Based on fluorine recovery, the fate of 11 percent of 42M-9 uptake remains unknown. The kinetics of uptake, metabolism and excretion of 42M-9 did not differ significantly over a five-fold change of inspired concentration. A comparison of the pulmonary clearance of unaltered 42M-9 and the fraction of uptake converted to urinary metabolites or unrecovered with those of other volatile halogenated anesthetics and their physical properties supports the conclusion that 42M-9 is relatively resistant to biotransformation.
1-溴-1,2,2-三氟环丁烷(42M-9)的物理性质与甲氧氟烷相似,有人建议将其用作麻醉剂。根据其脂溶性预测,其MAC值为0.26%。心血管或呼吸功能以及临床实验室检查均未观察到具有临床意义的变化。与其他人在麻醉浓度下报告的情况相比,本研究在镇痛浓度下未观察到室性心律失常。肺摄取率高且清除缓慢。呼出的总量占剂量的60%。相当于总摄取量11%的氟以非挥发性氟化代谢物的形式迅速经尿液排出。另外9%的42M-9降解为氟化物并经尿液排出。由于经尿液排出的氟化物量往往会沉积在骨骼中,大约29%的摄取量可能可归因于代谢物。基于氟的回收率,42M-9摄取量的11%的去向仍不清楚。在吸入浓度有五倍变化的情况下,42M-9的摄取、代谢和排泄动力学没有显著差异。将未改变的42M-9的肺清除率以及摄取转化为尿代谢物或未回收部分的比例与其他挥发性卤化麻醉剂的情况及其物理性质进行比较,支持了42M-9相对不易发生生物转化的结论。